WO2004066976A1 - Procede de production d'une forme pharmaceutique orale a decomposition immediate et liberation de principes actifs - Google Patents

Procede de production d'une forme pharmaceutique orale a decomposition immediate et liberation de principes actifs Download PDF

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Publication number
WO2004066976A1
WO2004066976A1 PCT/EP2003/013059 EP0313059W WO2004066976A1 WO 2004066976 A1 WO2004066976 A1 WO 2004066976A1 EP 0313059 W EP0313059 W EP 0313059W WO 2004066976 A1 WO2004066976 A1 WO 2004066976A1
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WO
WIPO (PCT)
Prior art keywords
acid
active ingredient
furosinopidic
copolymer
anionic
Prior art date
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PCT/EP2003/013059
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German (de)
English (en)
Inventor
Hans-Ulrich Petereit
Christian Meier
Andreas Gryczke
Original Assignee
Röhm GmbH & Co. KG
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Priority to ES03767591.5T priority Critical patent/ES2528359T3/es
Priority to BRPI0318049A priority patent/BRPI0318049B8/pt
Priority to JP2004567296A priority patent/JP5537756B2/ja
Priority to SI200332408T priority patent/SI1587497T1/sl
Priority to AU2003292061A priority patent/AU2003292061A1/en
Priority to EP03767591.5A priority patent/EP1587497B1/fr
Application filed by Röhm GmbH & Co. KG filed Critical Röhm GmbH & Co. KG
Priority to US10/542,283 priority patent/US8343542B2/en
Priority to MXPA05007643A priority patent/MXPA05007643A/es
Priority to CA2512738A priority patent/CA2512738C/fr
Publication of WO2004066976A1 publication Critical patent/WO2004066976A1/fr
Priority to IL169886A priority patent/IL169886A/en
Priority to US13/677,740 priority patent/US8999385B2/en

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Classifications

    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00—Medicinal preparations characterised by special physical form
    • A61K9/14—Particulate form, e.g. powders, Processes for size reducing of pure drugs or the resulting products, Pure drug nanoparticles
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61J—CONTAINERS SPECIALLY ADAPTED FOR MEDICAL OR PHARMACEUTICAL PURPOSES; DEVICES OR METHODS SPECIALLY ADAPTED FOR BRINGING PHARMACEUTICAL PRODUCTS INTO PARTICULAR PHYSICAL OR ADMINISTERING FORMS; DEVICES FOR ADMINISTERING FOOD OR MEDICINES ORALLY; BABY COMFORTERS; DEVICES FOR RECEIVING SPITTLE
    • A61J3/00—Devices or methods specially adapted for bringing pharmaceutical products into particular physical or administering forms
    • A61J3/10—Devices or methods specially adapted for bringing pharmaceutical products into particular physical or administering forms into the form of compressed tablets
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/185—Acids; Anhydrides, halides or salts thereof, e.g. sulfur acids, imidic, hydrazonic or hydroximic acids
    • A61K31/19—Carboxylic acids, e.g. valproic acid
    • A61K31/192—Carboxylic acids, e.g. valproic acid having aromatic groups, e.g. sulindac, 2-aryl-propionic acids, ethacrynic acid 
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K47/00—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
    • A61K47/06—Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite
    • A61K47/08—Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite containing oxygen, e.g. ethers, acetals, ketones, quinones, aldehydes, peroxides
    • A61K47/12—Carboxylic acids; Salts or anhydrides thereof
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00—Medicinal preparations characterised by special physical form
    • A61K9/0012—Galenical forms characterised by the site of application
    • A61K9/0053—Mouth and digestive tract, i.e. intraoral and peroral administration
    • A61K9/0056—Mouth soluble or dispersible forms; Suckable, eatable, chewable coherent forms; Forms rapidly disintegrating in the mouth; Lozenges; Lollipops; Bite capsules; Baked products; Baits or other oral forms for animals
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00—Medicinal preparations characterised by special physical form
    • A61K9/14—Particulate form, e.g. powders, Processes for size reducing of pure drugs or the resulting products, Pure drug nanoparticles
    • A61K9/141—Intimate drug-carrier mixtures characterised by the carrier, e.g. ordered mixtures, adsorbates, solid solutions, eutectica, co-dried, co-solubilised, co-kneaded, co-milled, co-ground products, co-precipitates, co-evaporates, co-extrudates, co-melts; Drug nanoparticles with adsorbed surface modifiers
    • A61K9/146—Intimate drug-carrier mixtures characterised by the carrier, e.g. ordered mixtures, adsorbates, solid solutions, eutectica, co-dried, co-solubilised, co-kneaded, co-milled, co-ground products, co-precipitates, co-evaporates, co-extrudates, co-melts; Drug nanoparticles with adsorbed surface modifiers with organic macromolecular compounds
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00—Medicinal preparations characterised by special physical form
    • A61K9/14—Particulate form, e.g. powders, Processes for size reducing of pure drugs or the resulting products, Pure drug nanoparticles
    • A61K9/16—Agglomerates; Granulates; Microbeadlets ; Microspheres; Pellets; Solid products obtained by spray drying, spray freeze drying, spray congealing,(multiple) emulsion solvent evaporation or extraction
    • A61K9/1605—Excipients; Inactive ingredients
    • A61K9/1629—Organic macromolecular compounds
    • A61K9/1641—Organic macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds, e.g. polyethylene glycol, poloxamers
    • A61K9/1647—Polyesters, e.g. poly(lactide-co-glycolide)
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00—Medicinal preparations characterised by special physical form
    • A61K9/20—Pills, tablets, discs, rods
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00—Medicinal preparations characterised by special physical form
    • A61K9/20—Pills, tablets, discs, rods
    • A61K9/2004—Excipients; Inactive ingredients
    • A61K9/2022—Organic macromolecular compounds
    • A61K9/205—Polysaccharides, e.g. alginate, gums; Cyclodextrin
    • A61K9/2054—Cellulose; Cellulose derivatives, e.g. hydroxypropyl methylcellulose
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/04—Antibacterial agents

Definitions

  • the invention relates to a method for producing an oral dosage form with immediate disintegration and active ingredient release already in the mouth.
  • the invention further relates to an active ingredient-containing powder and its use.
  • EP-A 0 417 588 describes a process for producing a complexed medicament from an ionogenic active substance by reacting the active substance with a complementary ionogenic, particulate polymer in the presence of a sufficient amount of water to moisten the mixture.
  • active ingredient salts it is necessary to add an acid or base to the mixture in order to neutralize the counter ion of the active ingredient.
  • active ingredient salts such as propranolol-HCl, verapamil-HCl or metoclopramide-HCl with anionic (meth) acrylate copolymers such as EUDRAGIT® L or EUDRAGIT® L100-55
  • sodium carbonate is added to the mixture, for example.
  • a particulate polymer can be used which has pendant amino groups as complementary ionogenic groups.
  • the pendant amino groups can e.g. B. a tertiary amino group, derived from polymerized monomers such. B. 2-Dimethylamino-ethyl methacrylate.
  • WO 01/39751 describes a process for the production of moldings by means of injection molding with the process steps a) melting a (meth) acrylate copolymer which is composed of 30 to 80% by weight of free-radically polymerized C1 to C4 alkyl esters of acrylic or Methacrylic acid and 70 to 20% by weight of (meth) acrylate monomers with a tertiary ammonium or amino group in the alkyl radical,
  • the (meth) acrylate copolymer being in a mixture with 1 to 70% by weight of a plasticizer and a drying agent in a ratio of 1: 1 to 1:20,
  • plasticizer at least 1% by weight of plasticizer is contained
  • the mixture may also contain further conventional additives or auxiliaries and, if appropriate, an active pharmaceutical ingredient, and the mixture, prior to melting, contains low-boiling components with a vapor pressure of at least 1.9 bar at 120 ° C. of more than 0.5% by weight having,
  • WO 02/67906 describes a process for the preparation of a coating and binder for oral or dermal pharmaceutical forms consisting essentially of (a) a copolymer consisting of free-radically polymerized C1 to C4 esters of acrylic or methacrylic acid and further (meth) acrylate Monomers which have functional tertiary ammonium groups, the copolymer being in powder form with an average particle size of 1-40 ⁇ m, (b) 3 to 15% by weight, based on (a), of an emulsifier with an HLB value of at least 14 and (c) 5 to 50% by weight, based on (a), a C 12 - to C 8 -monocarboxylic acid or a C12- to cis-hydroxyl compound, the components (a), (b) and (c ) are mixed or mixed with or without the addition of water and, if appropriate, with the addition of a pharmaceutical active ingredient and other customary additives, and the coating and binding agent are mixed from the mixture by melting, pouring, spreading
  • storage forms that are particularly stable are available, which contain, in particular, moisture-sensitive active ingredients such as acetylsalicylic acid, carbenoxolone, cefalotin, epinefrin, imipramine, potassium iodide, ketoprofen, levodopa, nitritrazepam, nitroprusside, oxitetracycline or benzimidazole derivative or HCIepazoline derivative, HCIepazoline derivative, or HCIepazoline derivative, or HCIepazoline derivative, or HCIepazoline derivative, or HCIepazoline derivative can.
  • moisture-sensitive active ingredients such as acetylsalicylic acid, carbenoxolone, cefalotin, epinefrin, imipramine, potassium iodide, ketoprofen, levodopa, nitritrazepam, nitroprusside, oxitetracycline or benzimidazole
  • Active ingredient classes and substances which can often cause bitter taste and which can advantageously also be formulated in a taste-isolating manner with the coating and binding agents according to WO 02/67906 e.g.
  • analgesics and anti-inflammatory drugs paracetamol, diclofenac, aceclofenac, ibuprofen, ketoprofen, flubiprofen, levacetylmethadol, oxycodone psychotropic drugs: prometazine, donepezil, modafinil, nefazodone, reboxetine, sertalin, sertraline
  • Antibiotics Ervthromicvn. Roxithromycin, clarithromycin, grepafloxacin,
  • Ciprofloxacin Ciprofloxacin, levofloxacin, sparfloxacin, trovafloxacin, nevirapine
  • Beta blockers propanolol, metoprolol, bisoprolol, nebivolol
  • Antidiabetic drugs metformin, miglitol, repaglinide
  • H1 antihistamines diphenhydramine, fexofenadine, mizolastine
  • H2 antihistamines cimetidine, nizatidine, ticlopidine, cetridine, ranitidine,
  • Vitamins thiamine nitrates: as well as other active ingredients: quinidine sulfate, amiloprilose HCI, pseudoephedrine
  • HCI sildenafil, topiramate, granisetron, rebamipids, quinine HCI
  • a problem with many oral dosage forms is that swallowing often involves the use of liquid, e.g. B. a sip of water required. This is unfavorable if no drink is available when needed or if the current professional activity has to be interrupted in order to be able to take the medication. For many patients, it is also uncomfortable to observe in the presence of other people and to take their medication, which is all the more noticeable when it is necessary to use a drink or even to request it for this purpose.
  • liquid e.g. B. a sip of water required.
  • a pharmaceutical form should be provided which can be taken without liquid and which releases the active ingredient immediately. There should be no sandy mouth taste.
  • the pharmaceutical form is said to be suitable for a large number of active ingredients, but in particular for pain relievers of the class of anti-rheumatic drugs or for antibiotics.
  • the invention relates to a method for producing an oral pharmaceutical form with immediate disintegration and active ingredient release already in the mouth, by intensive mixing
  • the anionic pharmaceutical active ingredient due to the production in the melt, is embedded in the copolymer in the form of a "solid solution".
  • the quantitative ratio based on% by weight of active ingredient to copolymer is advantageously from 2 to 1 to 1 to 2.
  • the copolymer is preferably present in equal amounts or in excess.
  • the anionic active ingredient (a) is preferably an anionic pain reliever, an anionic anti-rheumatic or an anionic antibiotic.
  • the active ingredient-containing powder can, for. B. contain the following anionic active ingredient:
  • copolymers (a) consist essentially or entirely of free-radically polymerized C1 to C4 esters of acrylic or methacrylic acid and further (meth) acrylate monomers which have functional tertiary amino groups. Suitable monomers with functional tertiary amino groups are listed in US Pat. No. 4,705,695, column 3, line 64 to column 4, line 13.
  • dimethylaminoethyl acrylate 2-dimethylaminopropyl acrylate, dimethylaminopropyl methacrylate, dimethylaminobenzyl acrylate, dimethylaminobenzyl methacrylate, (3-dimethylamino-2,2-dimethyl) propyl acrylate, dimethylamino-2,2-dimethyl) propyl methacrylate, (3-diethylamyl) propyl acrylate and diethylamino-2,2-dimethyl) propyl methacrylate.
  • Dimethylaminoethyl methacrylate is particularly preferred.
  • the content of the monomers with tertiary amino groups in the copolymer can advantageously be between 30 and 70% by weight, preferably between 40 and 60% by weight.
  • the proportions of the C1 to C4 esters of acrylic or methacrylic acid is 70-30% by weight. Mention should be made of methyl methacrylate, ethyl methacrylate, butyl methacrylate, methyl acrylate, ethyl acrylate, butyl acrylate.
  • a (meth) acrylate copolymer with tertiary amino groups corresponding to component (b) may, for. B. from 20-30% by weight methyl methacrylate, 20-30% by weight butyl methacrylate and 60-40% by weight dimethylaminoethyl methacrylate.
  • the proportion of component (a) in the formulation is preferably 50-90% by weight.
  • copolymers (b) are obtained in a manner known per se by radical substance, solution, bead or emulsion polymerization. Before processing, they must be brought into a suitable particle size range using suitable grinding, drying or spraying processes. Granules and powders are suitable. Suitable commercial products are e.g. B. EUDRAGIT® E 100 (granulate) or EUDRAGIT® E PO (powder). Component (c)
  • Component (c) 5 to 50, preferably 10 to 20% by weight (based on the copolymer component (b) of a C12 to C 2 2 -carboxylic acid.
  • Component (c) is important for processability. Preferred are unbranched C12 to C22 monocarboxylic acids, branched derivatives of the substances mentioned may also be suitable, if appropriate.
  • C1 2 to C 22 monocarboxylic acids are, in particular, lauric acid and myristic acid. Palmitic acid and stearic acid are preferred.
  • Emulsifiers with an HLB value of at least 14 should be less than 3% by weight, preferably less than 2 or 1% by weight, and in particular should not contain such an emulsifier.
  • the reason for this lies in the powder structure of the starting material, in which the inherent taste of such emulsifiers is particularly evident.
  • using the special method according to the invention it is possible to do without the emulsifier.
  • Emulsifiers or surfactants are surface-active substances with a lyobipolar character, ie their molecule must have non-polar, lipophilic and polar, hydrophilic centers (PH List, Arzneiffenformlehre, Erasmusliche Verlagsgesellschaft mbH Stuttgart, 1982, Chapter 6.2.). Depending on the molecular structure, a distinction is made between ionogenic and nonionic emulsifiers.
  • the HLB value is a measure of the hydrophilicity or lipophilicity of nonionic surfactants introduced by Griffin in 1950. It can be determined experimentally using the Marszall phenol titration method; see. "Perfumery, Cosmetics", Volume 60, 1979, pp. 444-448; further references in Römpp, Chemie-Lexikon, 8th ed. 1983, p.1750. See also z. B. U.S. 4,795,643 (Seth)).
  • HLB value hydrophilic / lipophilic balance
  • Emulsifiers with an HLB value above 14 are understood to be hydrophilic, non-ionic emulsifiers with an HLB range of at least 14 and also hydrophilic, anionic emulsifiers and their salts, which have a calculated HLB value above 14.
  • emulsifiers with an HLB value above 14 are e.g. B. sodium lauryl sulfate and sodium cetyl stearyl sulfate, sucrose stearate and polysorbate 80.
  • Pharmaceutical excipients with HLB values less than 14, such as. B. Glycerol monostearate, however, can also be contained in amounts of more than 3 wt .-%.
  • the powder is embedded in a water-soluble matrix made of customary pharmaceutical excipients.
  • the water-soluble matrix is mainly formed from fillers and binders. These are preferably z.
  • HPMC hydroxypropylmethyl cellulose
  • additives can e.g. B. release agents, pigments, stabilizers, antioxidants, pore formers, penetration enhancers, flavorings or flavorings. They serve as processing aids and are intended to ensure a safe and reproducible manufacturing process and good long-term storage stability, or they achieve additional advantageous properties in the pharmaceutical form.
  • Release agents generally have lipophilic properties and are usually added to the spray suspensions. They prevent ejoe agglomeration of the cores during filming.
  • Talc, Mg or Ca - are preferred Stearate, ground silica, kaolin or non-ionic emulsifiers with an HLB value between 3 and 8 are used.
  • Usual amounts used for release agents in the coating and binding agents according to the invention are between 0.1 to 10% by weight, based on the pharmaceutical form.
  • pigments in the coating and binding agents according to the invention are between 1 and 10% by weight, based on the pharmaceutical form.
  • additives can also be plasticizers. Usual amounts are between 0 and 50, preferably 0 to 20, in particular 0 to 10% by weight. However, it is particularly preferred to contain at most 5% by weight or no plasticizer, since the formulations are often already sufficiently elastic due to the presence of components (c) and additional plasticizers can lead to undesirable tackiness.
  • plasticizers can influence the functionality of the polymer layer. Plasticizers achieve a lowering of the glass transition temperature through physical interaction with the polymer and, depending on the amount added, promote film formation. Suitable substances usually have one Molecular weight between 100 and 20,000 and contain one or more hydrophilic groups in the molecule, e.g. B. hydroxyl, ester or amino groups.
  • plasticizers examples include citric acid alkyl esters, glycerol esters, alkyl phthalates, alkyl sebacates, succrose esters, sorbitan esters, diethyl sebacate, dibutyl sebacate and polyethylene glycols 200 to 12,000.
  • Preferred plasticizers are triethyl citrate (TEC), acetyl triethyl citrate (ATEC) and dibutyl sebacate (DBS).
  • esters which are liquid at room temperature such as citrates, phthalates, sebacates or castor oil, are also to be mentioned.
  • Citric acid and sebacic acid esters are preferably used. Mixtures of plasticizers can also be used.
  • the process according to the invention provides for the production of an oral pharmaceutical form with immediate disintegration and active ingredient release already in the mouth, by intensive mixing of components (a), (b) and (c) in the melt. Processing temperatures in the range from 80 to 200 ° C., preferably from 100 to 180 ° C., are suitable.
  • a twin-screw extruder is preferably used for the purpose of intensive mixing in the melt.
  • the mixture is ground to an active ingredient powder.
  • the average grain size of the powder should be 200 ⁇ m or less, preferably 50 to 150 ⁇ m.
  • the average grain or particle size of the powder can be determined as follows: by air jet sieving for easy division of the ground product into a few fractions. In this measuring range, this method is somewhat less precise than the alternatives. At least 70, preferably 90% of the particles based on however, the mass (mass distribution) should be in the size range according to the invention of 200 ⁇ m or less, preferably from 50 to 150 ⁇ m.
  • a very suitable measuring method is laser diffraction to determine the grain size distribution.
  • Commercial devices allow measurement in air (Malvern S3.01 particle sizer) or preferably in liquid media (LOT, Galai CIS 1). Precondition for the measurement in liquids is that the polymer does not dissolve in it or that the particles change in another way during the measurement.
  • a suitable medium is e.g. B. a highly diluted (about 0.02%) aqueous polysorbate 80 solution.
  • the active ingredient-containing powder can be processed into a tablet, lozenge, freeze-dried tablets, poured tablets or lozenges, sachets, chewable tablets, dry juices, candies and / or liquid-filled candies.
  • the active ingredient-containing copolymer powder is mixed with pharmaceutical excipients and can e.g. B. be pressed directly into tablets, lozenges or chewable tablets. The mixture can also be pasted with water, filled into a mold and freeze-dried so that freeze-dried tablets are obtained.
  • Cast tablets or lozenges can be obtained by using the active ingredient-containing copolymer powder, e.g. B. mixes with a saccharide solution at elevated temperature, poured into a mold, eg for tablets or candies, and solidifies by cooling.
  • Liquid-filled candies can be produced by adding a liquid mixture containing the active ingredient-containing copolymer powder e.g. B. in a sugar solution in a solid shell from z. B. injects a sugar and then closes it.
  • Active ingredient powder e.g. B. be pressed directly into tablets, lozenges or chewable tablets.
  • the mixture can also be pasted with water, filled into a mold and freeze-dried so that freeze-
  • the active ingredient-containing powder has an average grain size of 200 ⁇ m or less, preferably 50 to 150 ⁇ m, and contains
  • the active ingredient-containing powder can be used for the production of an oral pharmaceutical form with immediate disintegration and active ingredient release in the mouth, which after release has no bitter taste for at least 30 seconds.
  • the pharmaceutical form can be in the form of compressed tablets or lozenges, freeze-dried tablets, poured tablets or lozenges, sachets, chewable tablets, dry juices, candies and / or liquid-filled candies.
  • the taste isolation can be checked organoleptically in a simple manner by tasting. In this test, no or slightly bitter taste should be perceptible for at least 30 seconds after the active ingredient has been released. The determination of bitter values is more precise. No or slightly bitter taste corresponds to bitter values below 1000. Bitter values can be determined according to DAB 1999 method 2.8.N8 (determination of the bitter value).
  • the value according to the invention for an embedded anionic active ingredient is generally less than 1000, preferably less than 100.
  • a bitter value of 1000 is generally sufficient for pharmaceutical practice.
  • EUDRAGIT® E PO copolymer powder of methyl methacrylate, butyl methacrylate, and dimethylaminoethyl methacrylate in a ratio of 25: 25: 50 with a medium
  • EUDRAGIT® E 100 copolymer of methyl methacrylate, butyl methacrylate, and
  • Dimethylaminoethyl methacrylate in a ratio of 25: 25: 50 in the form of granules is a ratio of 25: 25: 50 in the form of granules.
  • the effectiveness of the taste isolation was tested organoleptically by tasting. The time between ingestion in the mouth and appearance of the bitter taste was determined.
  • Measuring kneader removed and cooled with dry ice.
  • Comparative Example 6 (active ingredient caffeine not of the invention) Compound 1 mol dimethylaminoethyl methacrylate units contained in the copolymer EUDRAGIT® E PO: 0.5 mol of stearic acid: 1.58 mol caffeine (F p: 234-239 ° C). 41.47 g of EUDRAGIT ® E PO, 18.53 g of stearic acid, 40 g of caffeine were weighed out and placed together in the IKA measuring kneader preheated to 100 ° C., where the mixture was at 100 ° C. product temperature for 20 min at 60 rpm (2 kneading blades) was kneaded. The mixture was removed from the kneader and cooled with dry ice. If you put 1 g of this compound in your mouth, it tastes bitter after 10 s.
  • Comparative Example 8 (active ingredient paracetamol not of the invention) Compound 1 mol dimethylaminoethyl methacrylate units contained in the copolymer EUDRAGIT® E PO: 0.5 mol of stearic acid: 2.03 mol paracetamol (F p: 168-172 ° C).
  • Comparative Example 9 (Paracetamol active ingredient not according to the invention) Compound with 1 mol of dimethylaminoethyl methacrylate units contained in the copolymer EUDRAGIT® E: 0.5 mol of stearic acid: 1 mol of paracetamol.
  • Copolymer EUDRAGIT® E PO 0.06 mol stearic acid: 0.77 mol ibuprofen.
  • Copolymer EUDRAGIT® E PO 0.12 mol stearic acid: 0.77 mol ibuprofen.
  • 100 g of EUDRAGIT ® E PO, 10 g of stearic acid and 50 g of ibuprofen were weighed out and put together in the IKA measuring kneader preheated to 100 ° C., where the mixture was at 100 ° C. product temperature for 20 min at 60 rpm (2 kneading blades) was kneaded. The mixture was removed from the kneader and cooled with dry ice. If you put 1 g of this compound in your mouth, it tastes bitter after 1 min.
  • Comparative Example 12 (Ci2-alcohol compound instead of stearic acid) Compound with 1 mol of dimethylaminoethyl methacrylate units contain in the copolymer EUDRAGIT® E PO: 0.34 mol dodecanol: 0.77 mol ibuprofen.
  • 100 g EUDRAGIT ® E PO, 20 g dodecanol and 50 g ibuprofen were weighed out and put together in the IKA measuring kneader preheated to 100 ° C., where the mixture at 100 ° C. product temperature for 20 min at 60 rpm (2 kneading blades) was kneaded. The mixture was removed from the kneader and cooled with dry ice.

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  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)

Abstract

L'invention concerne un procédé de production d'une forme pharmaceutique orale à décomposition immédiate et libération de principes actifs déjà dans la bouche par le mélange intensif (a) d'un principe actif pharmaceutique anionique avec (b) un copolymère, composé d'esters C1 à C4 à polymérisation radicalaire de l'acide acrylique ou méthacrylique et d'autres monomères de (méth)acrylate, possédant des groupes amino tertiaires fonctionnels, et (c) 5 à 50 % en poids, par rapport au (b), d'un acide carboxylique C12 à C22 dans la masse fondue, solidification du mélange et broyage en une poudre à teneur en principes actifs présentant une grosseur de grain moyenne inférieure ou égale à 200 µm, enrobage de la poudre dans une matrice soluble dans l'eau constituée d'adjuvants pharmaceutiques habituels, dans la mesure où pas plus de 3 % en poids, par rapport au copolymère, d'émulsifiants présentant une valeur HLB d'au moins 14 doivent être contenus. Ladite invention concerne également la poudre à teneur en principes actifs et ses applications.
PCT/EP2003/013059 2003-01-28 2003-11-21 Procede de production d'une forme pharmaceutique orale a decomposition immediate et liberation de principes actifs WO2004066976A1 (fr)

Priority Applications (11)

Application Number Priority Date Filing Date Title
BRPI0318049A BRPI0318049B8 (pt) 2003-01-28 2003-11-21 processo para produção de uma forma farmacêutica oral com imediata desintegração e liberação de ingrediente ativo, pó contendo ingrediente ativo e seu uso
JP2004567296A JP5537756B2 (ja) 2003-01-28 2003-11-21 直接崩壊し、かつ作用物質を放出する経口薬剤形を製造するための方法
SI200332408T SI1587497T1 (sl) 2003-01-28 2003-11-21 Postopek izdelave takoj razgradljive oralne farmacevtske oblike, ki sprosti aktivne učinkovine
AU2003292061A AU2003292061A1 (en) 2003-01-28 2003-11-21 Method for producing an immediately decomposing oral form of administration which releases active ingredients
EP03767591.5A EP1587497B1 (fr) 2003-01-28 2003-11-21 Procede de production d'une forme pharmaceutique orale a decomposition immediate et liberation de principes actifs
ES03767591.5T ES2528359T3 (es) 2003-01-28 2003-11-21 Procedimiento para la producción de una forma medicamentosa oral con desintegración y puesta en libertad inmediatas de las sustancias activas
US10/542,283 US8343542B2 (en) 2003-01-28 2003-11-21 Method for producing an immediately decomposing oral form of administration which releases active ingredients
MXPA05007643A MXPA05007643A (es) 2003-01-28 2003-11-21 Metodo para producir una forma farmaceutica oral con desintegracion inmediata y liberacion de ingrediente activo.
CA2512738A CA2512738C (fr) 2003-01-28 2003-11-21 Procede de production d'une forme pharmaceutique orale a decomposition immediate et liberation de principes actifs
IL169886A IL169886A (en) 2003-01-28 2005-07-26 Method for producing an immediately decomposing oral form of administration which releases active ingredients
US13/677,740 US8999385B2 (en) 2003-01-28 2012-11-15 Method for producing an immediately decomposing oral form of administration which releases active ingredients

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DE10304403A DE10304403A1 (de) 2003-01-28 2003-01-28 Verfahren zur Herstellung einer oralen Arzneiform mit unmittelbarem Zerfall und Wirkstofffreisetzung
DE10304403.5 2003-01-28

Related Child Applications (2)

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US10542283 A-371-Of-International 2003-11-21
US13/677,740 Continuation US8999385B2 (en) 2003-01-28 2012-11-15 Method for producing an immediately decomposing oral form of administration which releases active ingredients

Publications (1)

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WO2004066976A1 true WO2004066976A1 (fr) 2004-08-12

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PCT/EP2003/013059 WO2004066976A1 (fr) 2003-01-28 2003-11-21 Procede de production d'une forme pharmaceutique orale a decomposition immediate et liberation de principes actifs

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US (2) US8343542B2 (fr)
EP (1) EP1587497B1 (fr)
JP (2) JP5537756B2 (fr)
KR (1) KR100983461B1 (fr)
AU (1) AU2003292061A1 (fr)
BR (1) BRPI0318049B8 (fr)
CA (1) CA2512738C (fr)
DE (1) DE10304403A1 (fr)
ES (1) ES2528359T3 (fr)
IL (1) IL169886A (fr)
MX (1) MXPA05007643A (fr)
PL (1) PL206413B1 (fr)
SI (1) SI1587497T1 (fr)
WO (1) WO2004066976A1 (fr)

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WO2007028978A2 (fr) * 2005-09-06 2007-03-15 Selamine Ltd Et Al Formulation de ramipril
CN100336816C (zh) * 2005-12-14 2007-09-12 广州大学 一种舒巴坦制备方法
CN100402030C (zh) * 2006-01-05 2008-07-16 珠海联邦制药股份有限公司 一种含阿莫西林的药物组合物及其制备方法
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CN104784125A (zh) * 2015-04-14 2015-07-22 海南皇隆制药股份有限公司 一种注射用萘普生钠冻干粉针制剂及其制备方法
US9872906B2 (en) 2013-03-15 2018-01-23 Merck Sharp & Dohme Corp. Ceftolozane antibiotic compositions
CN109364777A (zh) * 2018-10-25 2019-02-22 瑞阳制药有限公司 美洛西林钠和舒巴坦钠混粉的制备方法及装置
US10376496B2 (en) 2013-09-09 2019-08-13 Merck, Sharp & Dohme Corp. Treating infections with ceftolozane/tazobactam in subjects having impaired renal function

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AR072777A1 (es) 2008-03-26 2010-09-22 Cephalon Inc Formas solidas de clorhidrato de bendamustina
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US8303989B2 (en) 2000-06-21 2012-11-06 International Health Management Associates, Inc. Compositions and methods for increasing the oral absorption of antimicrobials
US7527807B2 (en) 2000-06-21 2009-05-05 Cubist Pharmaceuticals, Inc. Compositions and methods for increasing the oral absorption of antimicrobials
WO2006118948A3 (fr) * 2005-04-29 2007-05-18 Cubist Pharm Inc Compositions therapeutiques
US8968781B2 (en) 2005-04-29 2015-03-03 Cubist Pharmaceuticals, Inc. Therapeutic compositions
WO2006118948A2 (fr) * 2005-04-29 2006-11-09 Cubist Pharmaceuticals, Inc. Compositions therapeutiques
WO2007028978A2 (fr) * 2005-09-06 2007-03-15 Selamine Ltd Et Al Formulation de ramipril
WO2007028978A3 (fr) * 2005-09-06 2007-09-07 Selamine Ltd Formulation de ramipril
CN100336816C (zh) * 2005-12-14 2007-09-12 广州大学 一种舒巴坦制备方法
CN100402030C (zh) * 2006-01-05 2008-07-16 珠海联邦制药股份有限公司 一种含阿莫西林的药物组合物及其制备方法
DE102007026550A1 (de) 2007-06-08 2008-12-11 Bayer Healthcare Ag Extrudate mit verbesserter Geschmacksmaskierung
WO2011141192A1 (fr) 2010-05-10 2011-11-17 Evonik Röhm Gmbh Forme posologique pharmaceutique comprenant un ou plusieurs principes actifs antirétroviraux
CN102078322A (zh) * 2011-02-17 2011-06-01 武汉同源药业有限公司 注射用哌拉西林钠他唑巴坦钠的医药用途
US8476425B1 (en) 2012-09-27 2013-07-02 Cubist Pharmaceuticals, Inc. Tazobactam arginine compositions
US9872906B2 (en) 2013-03-15 2018-01-23 Merck Sharp & Dohme Corp. Ceftolozane antibiotic compositions
US8968753B2 (en) 2013-03-15 2015-03-03 Calixa Therapeutics, Inc. Ceftolozane-tazobactam pharmaceutical compositions
US9044485B2 (en) 2013-03-15 2015-06-02 Calixa Therapeutics, Inc. Ceftolozane antibiotic compositions
US9320740B2 (en) 2013-03-15 2016-04-26 Merck Sharp & Dohme Corp. Ceftolozane-tazobactam pharmaceutical compositions
US9925196B2 (en) 2013-03-15 2018-03-27 Merck Sharp & Dohme Corp. Ceftolozane-tazobactam pharmaceutical compositions
US10420841B2 (en) 2013-03-15 2019-09-24 Merck, Sharp & Dohme Corp. Ceftolozane antibiotic compositions
US11278622B2 (en) 2013-03-15 2022-03-22 Merck Sharp & Dohme Corp. Ceftolozane antibiotic compositions
US10376496B2 (en) 2013-09-09 2019-08-13 Merck, Sharp & Dohme Corp. Treating infections with ceftolozane/tazobactam in subjects having impaired renal function
US10933053B2 (en) 2013-09-09 2021-03-02 Merck Sharp & Dohme Corp. Treating infections with ceftolozane/tazobactam in subjects having impaired renal function
US8906898B1 (en) 2013-09-27 2014-12-09 Calixa Therapeutics, Inc. Solid forms of ceftolozane
CN104784125A (zh) * 2015-04-14 2015-07-22 海南皇隆制药股份有限公司 一种注射用萘普生钠冻干粉针制剂及其制备方法
CN109364777A (zh) * 2018-10-25 2019-02-22 瑞阳制药有限公司 美洛西林钠和舒巴坦钠混粉的制备方法及装置
CN109364777B (zh) * 2018-10-25 2021-08-06 瑞阳制药股份有限公司 美洛西林钠和舒巴坦钠混粉的制备方法及装置

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MXPA05007643A (es) 2005-09-30
JP2014159424A (ja) 2014-09-04
US20130071475A1 (en) 2013-03-21
KR100983461B1 (ko) 2010-09-27
IL169886A0 (en) 2007-07-04
JP5537756B2 (ja) 2014-07-02
EP1587497B1 (fr) 2014-11-12
SI1587497T1 (sl) 2015-03-31
US20060051412A1 (en) 2006-03-09
CA2512738A1 (fr) 2004-08-12
ES2528359T3 (es) 2015-02-09
PL206413B1 (pl) 2010-08-31
KR20050096952A (ko) 2005-10-06
AU2003292061A1 (en) 2004-08-23
BRPI0318049B8 (pt) 2021-05-25
US8999385B2 (en) 2015-04-07
EP1587497A1 (fr) 2005-10-26
DE10304403A1 (de) 2004-08-05
PL376483A1 (en) 2005-12-27
JP2006514660A (ja) 2006-05-11
CA2512738C (fr) 2013-08-13
US8343542B2 (en) 2013-01-01
IL169886A (en) 2010-11-30
BRPI0318049B1 (pt) 2018-04-03
BR0318049A (pt) 2005-12-20

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